Technician - Quality Assurance - Parenteral (m/w/d)

Eli Lilly Eli Lilly · Pharma · Alzey, Germany

This role is for a Technician in Quality Assurance for parenteral manufacturing at a new Eli Lilly production facility in Germany. The primary focus is on ensuring compliance with cGMP standards during the setup and operation of the facility, including material preparation, aseptic filling, and visual inspection. The role involves on-site quality monitoring, deviation management, batch release support, and GMP documentation.

What you'd actually do

  1. Sorge für ein sicheres Arbeitsumfeld und sicheres Arbeiten; unterstütze alle Gesundheits-, Sicherheits- und Umweltziele des Unternehmens und des Standorts.
  2. Sei Hauptansprechpartner für interne/externe Kunden und beantworte allgemeine Informationsanfragen in deinem Fachgebiet.
  3. Schule und coache Betriebs- und Supportpersonal in Qualitätsfragen.
  4. Unterstütze Produktionsaktivitäten vor Ort mit regelmäßiger Präsenz im zugewiesenen Produktionsbereich.
  5. Befolge gute Dokumentationspraktiken und halte dich an Standortverfahren.

Skills

Required

  • Vocational training in a scientific or technical field or Bachelor's degree in science, engineering, or a pharmaceutical-related field.
  • Knowledge of cGMP practices including good documentation practices, data integrity, and regulatory requirements.
  • Minimum 2 years of experience in the pharmaceutical industry, with specific QA or QC experience in production monitoring.
  • Strong attention to detail and ability to maintain quality systems.
  • Fluent in German, basic English skills.
  • Teamwork.
  • Ability to communicate with cross-functional teams, good verbal and written communication skills.
  • Ability to work independently with a high degree of self-responsibility.
  • Ability to prioritize and meet deadlines.

Nice to have

  • Experience in parenteral manufacturing environments (equipment/material preparation, formulation, aseptic filling and/or visual inspection).

What the JD emphasized

  • cGMP practices
  • QA or QC experience in production monitoring
  • parenteral production environments